In-silico analysis of deleterious non-synonymous SNPs in the human AVPR1a gene linked to autism

Abstract Single nucleotide polymorphisms are the most prevalent type of DNA variation occurring at a single nucleotide within the genomic sequence. The AVPR1a gene exhibits genetic polymorphism and is linked to neurological and developmental problems, including autism spectrum disorder. Due to the d...

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Bibliographic Details
Published in:BMC Genomics
Main Authors: Md. Delowar Kobir Jibon, Md. Asadul Islam, Md. Eram Hosen, Md. Omar Faruqe, Rashed Zaman, Uzzal Kumar Acharjee, Biswanath Sikdar, Yewulsew Kebede Tiruneh, Md. Khalekuzzaman, Motasim Jawi, Magdi E. A. Zaki
Format: Article
Language:English
Published: BMC 2025-05-01
Subjects:
Polymorphism
Mutation
NsSNP
Docking
Autism
AVPR1a
Online Access:https://doi.org/10.1186/s12864-025-11655-1

Internet

https://doi.org/10.1186/s12864-025-11655-1

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